Genetic Disease
Conditions
Brief summary
Collection of coded biomaterial and clinical data with patients consent for future research.
Detailed description
Collection of coded biomaterial and clinical data with patients consent for future research, with the purpose to indentify new gene mutation and prossibilities for treatment in the future.
Interventions
GENETICBiobanking of biomaterial for future genetic research.
Sponsors
Maastricht University Medical Center
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* New patients visiting the out patient clinic of the department of Clinical Genetics of the Maastricht University Medical Hospital * Withdrawal of body material for genetic diagnostics.
Exclusion criteria
* Patient does not understand the Dutch language.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Comparing genes to discover unknown functions | Genes will be sequenced and compared, within an expected average of 6 months. | The biobanked bio material and medical data can be used for future research to learn more about the function of genes. |
Countries
Netherlands
Contacts
Primary ContactI. Krapels, MD, PhD
Outcome results
None listed